Pancreatitis and cholangitis in IgG4-related disease: Two cases report

  • Nguyễn Anh Tuấn Bệnh viện Trung ương Quân đội 108
  • Thái Doãn Kỳ Bệnh viện Trung ương Quân đội 108
  • Nguyễn Văn Thái Bệnh viện Trung ương Quân đội 108
  • Nguyễn Văn Mạnh Bệnh viện Trung ương Quân đội 108
  • Nguyễn Tiến Thịnh Bệnh viện Trung ương Quân đội 108
  • Nguyễn Lâm Tùng Bệnh viện Trung ương Quân đội 108
  • Trần Văn Hải Bệnh viện Trung ương Quân đội 108
  • Mai Thanh Bình Bệnh viện Trung ương Quân đội 108
  • Lê Thị Trang Bệnh viện Trung ương Quân đội 108

Main Article Content

Keywords

Immunoglobulin G4-related disease, autoimmune pancreatitis (AIP), IgG4-related sclerosing cholangitis (IgG4-SC)

Abstract

Immunoglobulin G4-related disease is an immune-mediated fibroinflammatory condition that can affect multiple organs. We report two cases of IgG4-RD diagnosed by imaging, serum IgG4 and histopathology. The first case was a 58-years-old male with a medical history of cholecystectomy and pancreatic pseudocyst drainage surgery who presented with symptoms of biliary obstruction and recurrent pancreatitis. CT/MRI showed diffuse sausage-like swelling of the pancreas. The result of histopathology and serum IgG4 were typical of IgG4-RD and the patient rapidly responded to treatment of corticosteroid. The second case was a 77-years-old male with a medical history of idiopathic pancreatitis who presented with symptoms of biliary obstruction and acute recurrent pancreatitis. An abdominal CT scan showed diffuse sausage-like swelling of the pancreas, sclerosing cholangitis with thickening and enhancement of the common bile duct wall. Serum IgG4 level was highly elevated. The patient was diagnosed with IgG-RD and responded well to corticosteroid therapy. IgG4-RD is generally seen in males in their sixth to seventh decade of life and can involve one or multiple organs. It should be considered in patients presenting with suspect symptoms.

Article Details

References

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